Delamination resistant pharmaceutical glass containers containing active pharmaceutical ingredients
US-2015374582-A1 · Dec 31, 2015 · US
US9707155B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9707155-B2 |
| Application number | US-201414259286-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 23, 2014 |
| Priority date | Apr 24, 2013 |
| Publication date | Jul 18, 2017 |
| Grant date | Jul 18, 2017 |
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The present invention is based, at least in part, on the identification of a pharmaceutical container formed, at least in part, of a glass composition which exhibits a reduced propensity to delaminate, i.e., a reduced propensity to shed glass particulates. As a result, the presently claimed containers are particularly suited for storage of pharmaceutical compositions and, specifically, a pharmaceutical solution comprising a pharmaceutically active ingredient, for example, LYXUMIA (lixisenatide), LEMTRADA (alemtuzumab), REGN727/SAR236553 (alirocumab), SAR2405550/BSI-201 (iniparib), OTAMIXABAN (otamixaban), SARILUMAB (sarilumab), LANTUS and LYXUMIA (insulin glargine and lixisenatide) or VISAMERIN/MULSEVO (semuloparin sodium).
Opening claim text (preview).
What is claimed is: 1. A pharmaceutical product comprising: lixisenatide, alemtuzumab, alirocumab, iniparib, otamixaban, sarilumab, insulin glargine and lixisenatide or semuloparin sodium and a pharmaceutically acceptable excipient; contained within a glass pharmaceutical container comprising a glass composition comprising: SiO 2 in a an amount greater than or equal to about 72 mol. % and less than or equal to about 78 mol. %; alkaline earth oxide comprising both MgO and CaO, wherein CaO is present in an amount up to about 1.0 mol. %, and a ratio (CaO (mol. %)/(CaO (mol. %)+MgO (mol. %))) is less than or equal to 0.5; X mol. % Al 2 O 3 , wherein X is greater than or equal to about 5 mol. % and less than or equal to about 7 mol. %; Y mol. % alkali oxide, wherein the alkali oxide comprises Na 2 O in an amount greater than about 8 mol. %; and a ratio of a concentration of B 2 O 3 (mol. %) in the glass container to (Y mol. %-X mol. %) is less than or equal to 0.3. 2. The pharmaceutical product of claim 1 , wherein the pharmaceutical container comprises a compressive stress greater than or equal to 150 MPa. 3. The pharmaceutical product of claim 1 , wherein the pharmaceutical container comprises a compressive stress greater than or equal to 250 MPa. 4. The pharmaceutical product of claim 1 , wherein the pharmaceutical container comprises a depth of layer greater than 30 μm. 5. The pharmaceutical product of claim 1 , wherein the pharmaceutical product comprises increased stability, product integrity, or efficacy. 6. The pharmaceutical product of claim 1 : wherein the glass pharmaceutical container has a compressive stress greater than or equal to 150 MPa and a depth of layer greater than 10 μm, and wherein the pharmaceutical product comprises increased stability, product integrity, or efficacy. 7. The pharmaceutical product of claim 1 : wherein the glass pharmaceutical container which is substantially free of boron, and wherein the pharmaceutical product comprises increased stability, product integrity, or efficacy. 8. The pharmaceutical product of claim 7 , wherein the glass pharmaceutical container comprises a compressive stress greater than or equal to 150 MPa and a depth of layer greater than 25 μm. 9. The pharmaceutical product of claim 8 , wherein the glass pharmaceutical container comprises a compressive stress greater than or equal to 300 MPa and a depth of layer greater than 35 μm. 10. The pharmaceutical product of claim 7 , wherein said glass pharmaceutical container comprises a substantially homogeneous inner layer. 11. The pharmaceutical product of claim 10 , wherein said glass pharmaceutical container comprises a compressive stress greater than or equal to 150 MPa and a depth of layer greater than 25 μm. 12. The pharmaceutical product of claim 1 , wherein the pharmaceutical container comprises an internal homogeneous layer.
to perform ion-exchange between alkali ions (C03C21/005 takes precedence) · CPC title
Pyridinium derivatives, e.g. pralidoxime, pyridostigmine · CPC title
having the carbon of a carboxamide group directly attached to the aromatic ring, e.g. procainamide, procarbazine, metoclopramide, labetalol · CPC title
containing calcium oxide, e.g. common sheet or container glass · CPC title
IL-6 · CPC title
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